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Simultaneous Quantitative Assessment of Ochratoxin A, Patulin, 5-Hydroxymethylfurfural, and Bisphenol A in Fruit Drinks Using HPLC with Diode Array-Fluorimetric Detection

The analysis of regulated contaminants in fruit drinks often requires suitable validated and rapid analytical methods for cost-effective food control, and is of considerable interest among the fruit beverage industry. This study demonstrated a rapid and sensitive high-performance liquid chromatograp...

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Autores principales: Hassan, Norfarizah Hanim, Othman, Haneen Ibrahim Ahmad Al, Abdul Malek, Nur Rabiatutadawiah, Zulkurnain, Musfirah, Saad, Bahruddin, Wong, Yong Foo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7695309/
https://www.ncbi.nlm.nih.gov/pubmed/33182246
http://dx.doi.org/10.3390/foods9111633
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author Hassan, Norfarizah Hanim
Othman, Haneen Ibrahim Ahmad Al
Abdul Malek, Nur Rabiatutadawiah
Zulkurnain, Musfirah
Saad, Bahruddin
Wong, Yong Foo
author_facet Hassan, Norfarizah Hanim
Othman, Haneen Ibrahim Ahmad Al
Abdul Malek, Nur Rabiatutadawiah
Zulkurnain, Musfirah
Saad, Bahruddin
Wong, Yong Foo
author_sort Hassan, Norfarizah Hanim
collection PubMed
description The analysis of regulated contaminants in fruit drinks often requires suitable validated and rapid analytical methods for cost-effective food control, and is of considerable interest among the fruit beverage industry. This study demonstrated a rapid and sensitive high-performance liquid chromatography approach for the simultaneous determination of ochratoxin A (OTA), patulin (PAT), 5-hydroxymethylfurfural (HMF), and bisphenol A (BPA) in various fruit drinks. The separations were achieved using a C18 core-shell column with both photo-diode array and fluorimetric detections connected in series. A gradient system consisting of methanol and 0.1% formic acid at a flow rate of 1.2 mL min(−1), thermostated at 35 °C, provided fast elution with run time <9 min. Sample pretreatment was optimised to enable extraction of all analytes from fruit drink matrices. The optimised method was validated. Correlation coefficients of R > 0.99 were achieved with detection limits of 0.5 ng mL(−1) (OTA), 1.1 ng mL(−1) (PAT), 7.9 ng mL(−1) (HMF), and 1.0 ng mL(−1) (BPA). Recoveries ranged from 82% to 99%. Good relative standard deviations for intraday retention times (≤3.54%) and peak area (≤3.5%) were achieved. The developed multi-contaminants analysis method was successfully applied to determine OTA, PAT, HMF, and BPA in various fruit drinks.
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spelling pubmed-76953092020-11-28 Simultaneous Quantitative Assessment of Ochratoxin A, Patulin, 5-Hydroxymethylfurfural, and Bisphenol A in Fruit Drinks Using HPLC with Diode Array-Fluorimetric Detection Hassan, Norfarizah Hanim Othman, Haneen Ibrahim Ahmad Al Abdul Malek, Nur Rabiatutadawiah Zulkurnain, Musfirah Saad, Bahruddin Wong, Yong Foo Foods Article The analysis of regulated contaminants in fruit drinks often requires suitable validated and rapid analytical methods for cost-effective food control, and is of considerable interest among the fruit beverage industry. This study demonstrated a rapid and sensitive high-performance liquid chromatography approach for the simultaneous determination of ochratoxin A (OTA), patulin (PAT), 5-hydroxymethylfurfural (HMF), and bisphenol A (BPA) in various fruit drinks. The separations were achieved using a C18 core-shell column with both photo-diode array and fluorimetric detections connected in series. A gradient system consisting of methanol and 0.1% formic acid at a flow rate of 1.2 mL min(−1), thermostated at 35 °C, provided fast elution with run time <9 min. Sample pretreatment was optimised to enable extraction of all analytes from fruit drink matrices. The optimised method was validated. Correlation coefficients of R > 0.99 were achieved with detection limits of 0.5 ng mL(−1) (OTA), 1.1 ng mL(−1) (PAT), 7.9 ng mL(−1) (HMF), and 1.0 ng mL(−1) (BPA). Recoveries ranged from 82% to 99%. Good relative standard deviations for intraday retention times (≤3.54%) and peak area (≤3.5%) were achieved. The developed multi-contaminants analysis method was successfully applied to determine OTA, PAT, HMF, and BPA in various fruit drinks. MDPI 2020-11-09 /pmc/articles/PMC7695309/ /pubmed/33182246 http://dx.doi.org/10.3390/foods9111633 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hassan, Norfarizah Hanim
Othman, Haneen Ibrahim Ahmad Al
Abdul Malek, Nur Rabiatutadawiah
Zulkurnain, Musfirah
Saad, Bahruddin
Wong, Yong Foo
Simultaneous Quantitative Assessment of Ochratoxin A, Patulin, 5-Hydroxymethylfurfural, and Bisphenol A in Fruit Drinks Using HPLC with Diode Array-Fluorimetric Detection
title Simultaneous Quantitative Assessment of Ochratoxin A, Patulin, 5-Hydroxymethylfurfural, and Bisphenol A in Fruit Drinks Using HPLC with Diode Array-Fluorimetric Detection
title_full Simultaneous Quantitative Assessment of Ochratoxin A, Patulin, 5-Hydroxymethylfurfural, and Bisphenol A in Fruit Drinks Using HPLC with Diode Array-Fluorimetric Detection
title_fullStr Simultaneous Quantitative Assessment of Ochratoxin A, Patulin, 5-Hydroxymethylfurfural, and Bisphenol A in Fruit Drinks Using HPLC with Diode Array-Fluorimetric Detection
title_full_unstemmed Simultaneous Quantitative Assessment of Ochratoxin A, Patulin, 5-Hydroxymethylfurfural, and Bisphenol A in Fruit Drinks Using HPLC with Diode Array-Fluorimetric Detection
title_short Simultaneous Quantitative Assessment of Ochratoxin A, Patulin, 5-Hydroxymethylfurfural, and Bisphenol A in Fruit Drinks Using HPLC with Diode Array-Fluorimetric Detection
title_sort simultaneous quantitative assessment of ochratoxin a, patulin, 5-hydroxymethylfurfural, and bisphenol a in fruit drinks using hplc with diode array-fluorimetric detection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7695309/
https://www.ncbi.nlm.nih.gov/pubmed/33182246
http://dx.doi.org/10.3390/foods9111633
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